CAS: 99-90-1; 1-(4-Bromophenyl)Ethanone

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1-(4-bromophenyl)ethanol 3-(4-bromophenyl)-3-oxopropanoic acid bromobenzene acetic anhydride 4-piperidinoacetophenone 1-(2-(4-bromophenyl)-2-oxoethyl)pyridin-1-ium iodide (E)-1-(4-bromophenyl)-3-(furan-2-yl)-2-propen-1-one 2-(4-bromo-phenyl)-6-iodo-quinoline-4-carboxylic acid

4-溴茴香硫醚置于氧气体系中,用 乙腈 作为反应溶剂,化学反应 8.0H,反应生成 4-溴苯乙酮
参考文献:连接工程介导的载流子转移和氮化碳表面反应以提高光催化活性
标题:连接工程介导的载流子转移和氮化碳表面反应以提高光催化活性
摘要:合理调整具有多种功能的光催化剂的原子结构以提高载流子转移效率和氮化碳(c 3 N 4)的表面活化是有前途的,也是一个挑战.在这里,我们首次报道了通过将甲醛与蜜勒胺共聚,在功能性氮化碳 (Cocn) 中构建两亲碳和 C-O-C 链连接的末端蜜勒胺单元的简便策略.通过将碳和 C-O-C 链的两亲载流子桥整合到框架中,光生载流子迁移率和活性物质(超氧自由基,单线态氧)以及表面相互作用得到显着改善.因此,C 3 N 4的最佳剪裁在制氢 (34.9 μmol H-1) 和使用空气将硫化物选择性氧化为亚砜方面获得优异的光催化活性(光照 3 小时后转化率和选择性接近 100%),比原始 C 3 N高约 7 倍4 . 这项研究为有机基光催化剂上载流子转移和表面反应的原子定制提供了深入的见解和策略.
DOI:10.1039/d1Ta03813C

专利信息

专利号:US-2012215002-A1
优先权日:2009-10-09
标 题:Synthesis of optically active intermediate for the preparation of montelukast
发明人：LEFORT LAURENT
权利人:LEFORT LAURENT
摘要:The present invention relates to the synthesis of optically active alcohols by means of enantioselective hydrogenation of ketones in biphasic systems. In particular the present invention relates to the synthesis of an optically active alcohol of general formula (1).

专利号:US-11999757-B2
优先权日:2017-11-01
标 题:Synthesis of boronate ester derivatives and uses thereof
发明人：BOYER SERGE HENRI; HECKER SCOTT J; VERZIJL GERARDUS K M; HERMSEN PETRUS J
权利人:MELINTA SUBSIDIARY CORP
摘要:Disclosed herein are methods for the preparation of boronate derivatives in the synthesis of antimicrobial compounds and uses thereof. Disclosed herein includes method of making a compound of Formula (B) by reducing the ketone group of the keto-ester compound of Formula (A), and the reduction can be performed using a Ruthenium based catalyst system or using an alcohol dehydrogenase bioreduction system.

专利号:US-2007260076-A1
优先权日:2003-12-05
标 题:Practical, Cost-Effective Synthesis of Ubiquinones
发明人：LIPSHUTZ BRUCE H; BERL VOLKER; SHEIN KARIN; WETTERICH FRANK
权利人:LIPSHUTZ BRUCE H; BERL VOLKER; SHEIN KARIN; WETTERICH FRANK
摘要:The present invention provides a convergent method for the synthesis of ubiquinones and ubiquinone analogues. Also provided are precursors of ubiquinones and their analogues that are useful in the methods of the invention. The invention further provides an improved method for the carboalumination of alkyne substrates.

专利号:US-2006167289-A1
优先权日:2003-12-05
标题 :Practical, cost-effective synthesis of ubiquinones
发明人：LIPSHUTZ BRUCE H; BERL VOLKER; SCHEIN KARIN; WETTERICH FRANK
权利人:ZYMES LLC
摘要:The present invention provides a convergent method for the synthesis of ubiquinones and ubiquinone analogues. Also provided are precursors of ubiquinones and their analogues that are useful in the methods of the invention. The invention further provides an improved method for the carboalumination of alkyne substrates.

专利号:US-10669292-B2
优先权日:2014-05-05
标 题 :Synthesis of boronate salts and uses thereof
发明人：HECKER SCOTT; BOYER SERGE
权利人:REMPEX PHARMACEUTICALS INC
摘要:Disclosed herein are boronate intermediates in the synthesis of antimicrobial compounds and the use and preparation thereof. Some embodiments relate to crystalline boronate salt derivatives and their use in the synthesis of therapeutic compounds.

专利号:US-5300638-A
优先权日:1991-07-31
标题:Asymmetric synthesis of taxol side chain
发明人：FARINA VITTORIO; HAUCK SHEILA I
权利人:BRISTOL MYERS SQUIBB CO
摘要:The present invention relates to a process for the preparation of (3R, 4S)-3-hydroxy-4-phenyl-2-azetidinone derivatives which are useful intermediates in the synthesis of taxol from baccatin III, said process comprises reacting an acyloxyacetyl halide with an imine derived from L-threonine; and to compounds of formula (III) which are produced in said process: ##STR1## wherein Ar is phenyl; R 1 is hydrogen, an acyl radical of a carboxylic acid, or a carbonic acid ester radical; R 2 is hydrogen or a carboxy protecting group; and R 3 is hydrogen or a hydroxy protecting group.